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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1092692Generated: October 27, 2026

2-Butyn-1-ol → HCID 59341119, compound

https://huagongshe.com/reaction/1092692

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Butyn-1-olHCID 12991—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-(6-chloro-5-fluoropyrimidin-4-yl)-2-ethylhexahydro-1H-azepineHCID 59341131—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59341119HCID 5934111991.4%

Reaction Steps

0.07 g of sodium hydride (60% oil suspention) was suspended in 2 ml of tetrahydrofuran. 0.3 ml of tetrahydrofuran solution of 0.11 g of 2-butyn-1-ol was added dropwise at room temperature therein, and the mixture was stirred for 10 minutes. Into the mixture was added dropwise 0.3 ml of tetrahydrofuran solution of 0.30 g of 1-(6-chloro-5-fluoropyrimidin-4-yl)-2-ethyl-hexahydro-1H-azepine at room temperature, and stirred for 9 hours at 60° C. After the reaction mixture was cooled to near room temperature, the reaction mixture was poured into a saturated ammonium chloride aqueous solution, and the mixture was extracted with tert-butyl methyl ether three times. The organic layers were washed with a saturated sodium chloride aqueous solution, dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography to obtain 0.31 g of 1-(6-(2-butynyloxy)-5-fluoropyrimidin-4-yl)-2-ethyl-hexahydro-1H-azepine (hereinafter, referred to as Compound (50)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129526B2
Source datasetuspto-grants-2012_03
ORD IDord-c0b384719f414c7eb2d61833da4c9d16
Source noteuspto-grants-2012_03